Canonical Allele Identifier: CA6647150
Community Standard Title: NM_145064.3(STAC3):c.432+4A>T
Gene: STAC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57248702T>A , CM000674.2:g.57248702T>A GRCh38
NC_000012.11:g.57642485T>A , CM000674.1:g.57642485T>A GRCh37
NC_000012.10:g.55928752T>A NCBI36
NG_033835.1:g.7492A>T

Transcript Alleles

HGVS Amino-acid Change
NM_145064.3:c.432+4A>T MANE Select NP_659501.1:n.432+4A>T
ENST00000332782.7:c.432+4A>T MANE Select ENSP00000329200.2:n.432+4A>T
NM_001286256.1:c.315+4A>T NP_001273185.1:n.315+4A>T
NM_001286256.2:c.315+4A>T NP_001273185.1:n.315+4A>T
NM_001286257.1:c.-126-504A>T NP_001273186.1:n.-126-504A>T
NM_001286257.2:c.-126-504A>T NP_001273186.1:n.-126-504A>T
NM_145064.2:c.432+4A>T NP_659501.1:n.432+4A>T
NR_104422.1:n.202-504A>T
NR_104422.2:n.196-504A>T
ENST00000332782.6:c.432+4A>T ENSP00000329200.2:n.432+4A>T
ENST00000546246.2:c.-126-504A>T ENSP00000441515.2:n.-126-504A>T
ENST00000553489.1:c.432+4A>T ENSP00000452299.1:n.432+4A>T
ENST00000554578.5:c.315+4A>T ENSP00000452068.1:n.315+4A>T
ENST00000557176.5:c.-126-504A>T ENSP00000450740.1:n.-126-504A>T
XM_011538126.1:c.432+4A>T XP_011536428.1:n.432+4A>T
XM_011538126.2:c.432+4A>T XP_011536428.1:n.432+4A>T
XR_002957305.1:n.628+4A>T
XR_944515.1:n.628+4A>T
XR_944515.2:n.628+4A>T